Sodium hydride → 12-(tert-Butoxycarbonyl)-6,12-bis(benzyloxy)-7-oxo-6,12-diazadodecanenitrile

HRID 2380136Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2380136
[C:1]([O:5][C:6]([NH:8][O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].[CH2:19]([O:26][N:27]([CH2:35][CH2:36][CH2:37][CH2:38][C:39]#[N:40])[C:28](=[O:34])[CH2:29][CH2:30][CH2:31][CH2:32]Cl)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>CN(C=O)C>[C:1]([O:5][C:6]([N:8]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH2:32][CH2:31][CH2:30][CH2:29][C:28](=[O:34])[N:27]([O:26][CH2:19][C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)[CH2:35][CH2:36][CH2:37][CH2:38][C:39]#[N:40])=[O:7])([CH3:4])([CH3:2])[CH3:3]

Komponenten

5

Edukt 3

HCID 24758Sodium hydrideHCID 736159Tert-butyl N-(benzyloxy)carbamateHCID 10087530N-(Benzyloxy)-N-(4-cyanobutyl)-5-chloropentanamide

Produkt 1

HCID 1032403412-(tert-Butoxycarbonyl)-6,12-bis(benzyloxy)-7-oxo-6,12-diazadodecanenitrileAusbeute 77 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

N-(tert-Butoxycarbonyl)-O-benzylhydroxylamine (4.2 g, 18.8 mmol) was dissolved in DMF (120 mL) and cooled to 0° C. Sodium hydride (80%, 0.564 g, 18.8 mmol) was added, and the mixture was stirred at 0° C. for 30 minutes. A solution of (3) (6.0 g, 18.6 mmol) in DMF (30 mL) was slowly added to the cold solution which was then allowed to stir at room temperature for 20 minutes and at 80° C. overnight. The DMF was removed under high vacuum, and the reside was quenched with H2O (50 mL) and extracted with CH2Cl2 (3×70 mL). Organic extracts were washed with saturated sodium chloride, and the solvent was removed by rotary evaporation. Silica gel column chromatography, eluting with 2:1 hexane/EtOAc produced 7.29 g (77%) of (4) as an oil: NMR δ 1.50 (s, 9H), 1.40-1.90 (m, 8H), 2.30 (t, 2H, J=6), 2.40 (t, 2H, J=6), 3.40 (t, 2H, J=6), 3.63 (t, 2H, J=6), 4.77 (s, 2H), 4.80 (s, 2H), 7.33 (s, 10H) . Anal. (C29H39N3O5), C, H, N.

Aufarbeitung

  1. stirringto stir at room temperature for 20 minutes and at 80° C. overnight
  2. customThe DMF was removed under high vacuum
  3. customthe reside was quenched with H2O (50 mL)
  4. extractionextracted with CH2Cl2 (3×70 mL)
  5. washOrganic extracts were washed with saturated sodium chloride
  6. customthe solvent was removed by rotary evaporation
  7. washSilica gel column chromatography, eluting with 2:1 hexane/EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-d0cb78d5204e4249bf074898f6223c63
Quelldatensatz
uspto-grants-1994_11
Patentnummer
US05364965

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